The Role of Genomic Copy Number Variation in Regulation of Bone Disease Phenotypes

Wilson, Scott (Chief Investigator)
Prince, Richard (Investigator 02)

Status	Finished
Effective start/end date	1/01/11 → 31/12/13

Funding

National Health & Medical Research Council NHMRC: A$107,508.00
National Health & Medical Research Council NHMRC: A$143,205.00
National Health & Medical Research Council NHMRC: A$173,902.00

Access Project

http://purl.org/au-research/grants/nhmrc/1010494

2 Article

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
Mullin, B., Tickner, J., Zhu, K., Kenny, J., Mullin, S., Brown, S. J., Dudbridge, F., Pavlos, N., Mocarski, E. S., Walsh, J. P., Xu, J. & Wilson, S., 26 Mar 2020, In: Genome Biology. 21, 1, 80.
Research output: Contribution to journal › Article › peer-review

Open Access
11 Citations (Web of Science)
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes
Ruth, K. S., Campbell, P. J., Chew, S., Lim, E. M., Hadlow, N., Stuckey, B., Brown, S. J., Feenstra, B., Joseph, J., Surdulescu, G. L., Zheng, H. F., Richards, J. B., Murray, A., Spector, T. D., Wilson, S. & Perry, J. R. B., 2016, In: European Journal of Human Genetics. 24, 2, p. 284-290 7 p.
Research output: Contribution to journal › Article › peer-review

Open Access
56 Citations (Scopus)